Molecular characterization of Thai patients with phenylalanine hydroxylase deficiency and in vitro functional study of two novel PAH variants. Ngiwsara L, Vatanavicharn N*, Sawangareetrakul P, Liammongkolkul S, Ratanarak P, Boonyawat B, Srisomsap C, Champattanachai V, Ketudat-Cairns J, Wasant P, Svasti J. Mol Biol Rep. 2021 Mar;48(3):2063-2070.

Novel mutations found in two genes of thai patients with isolated methylmalonic acidemia. Keeratichamroen S, Cairns JR, Sawangareetrakul P, Liammongkolkul S, Champattanachai V, Srisomsap C, Kamolsilp M, Wasant P, Svasti J*. Biochem Genet. 2007 Jun;45(5-6):421-30.

Design, synthesis, biological evaluation and molecular modeling studies of novel naphthoquinone-triazole hybrids as potential FGFR1 tyrosine kinase inhibitors Leechaisit R, Mahalapbutr P, Suriya U, Sukonthasakorn P, Prachayasittikul V, Mandi P, Prachayasittikul S, Ruchirawat S, Prachayasittikul V, Pingaew R Asian J Org Chem. 2025;14(5):e202400813.